Nanoparticulate Tetrac Inhibits Growth and Vascularity of Glioblastoma Xenografts
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Thyroid hormone as L-thyroxine (T4) stimulates proliferation of glioma cells in vitro and medical induction of hypothyroidism slows clinical growth of glioblastoma multiforme (GBM). The proliferative action of T4 on glioma cells is initiated nongenomically at a cell surface receptor for thyroid hormone on the extracellular domain of integrin αvβ3. Tetraiodothyroacetic acid (tetrac) is a thyroid hormone derivative that blocks T4 action at αvβ3 and has anticancer and anti-angiogenic activity. Tetrac has been covalently bonded via a linker to a nanoparticle (Nanotetrac, Nano-diamino-tetrac, NDAT) that increases the potency of tetrac and broadens the anticancer properties of the drug. In the present studies of human GBM xenografts in immunodeficient mice, NDAT administered daily for 10 days subcutaneously as 1 mg tetrac equivalent/kg reduced tumor xenograft weight at animal sacrifice by 50%, compared to untreated control lesions (p < 0.01). Histopathological analysis of tumors revealed a 95% loss of the vascularity of treated tumors compared to controls at 10 days (p < 0.001), without intratumoral hemorrhage. Up to 80% of tumor cells were necrotic in various microscopic fields (p < 0.001 vs. control tumors), an effect attributable to devascularization. There was substantial evidence of apoptosis in other fields (p < 0.001 vs. control tumors). Induction of apoptosis in cancer cells is a well-described quality of NDAT. In summary, systemic NDAT has been shown to be effective by multiple mechanisms in treatment of GBM xenografts.
KeywordsThyroid Hormone Glioblastoma Xenograft Mouse GL261 Rodent Glioma GL261 Cell Line
Glioblastoma multiforme (GBM) is an aggressive central nervous system tumor with high mortality [1, 2]. The tumor is also relatively chemoresistant [3, 4] and radioresistant . Its invasiveness and asymmetry result in fewer than 30% of patients at presentation having tumors amenable to total resection . The cancer is highly vascular, causing the evaluation of anti-angiogenesis in its management . Against this background, it is understandable that a number of novel therapeutic approaches are under investigation [8, 9, 10].
Hercbergs and co-workers in a prospective, controlled clinical study developed evidence that GBM is thyroid hormone dependent, that is, medical induction of mild hypothyroidism slowed the course of the disease . We reported that thyroid hormone, L-thyroxine (T4), was a proliferative factor in vitro in rat C6 and F98 cells and mouse GL261 cell line models for glioblastoma . This effect was mediated by the cell surface thyroid hormone receptor we described on plasma membrane integrin αvβ3 [13, 14]. The deaminated T4 derivative, tetraiodothyroacetic acid (tetrac), blocked the proliferative action nongenomically initiated by T4 on these cells . We also demonstrated that thyroid hormone was anti-apoptotic in glioma cells . In studies of a human GBM cell line (U87MG), we defined discrete domains in the thyroid hormone receptor on αvβ3 that bound T3 and both T4 and T3 . The T3 domain activated phosphatidylinositol 3-kinase (PI3-K), whereas mitogen-activated protein kinase (MAPK; ERK1/2) signal transduction pathway was activated by the T4/T3 domain. The latter supported U87MG cell proliferation.
We subsequently showed in a variety of xenografts that a formulation of tetrac covalently linked to a nanoparticle (Nanotetrac, Nano-diamino-tetrac, NDAT)—an agent thus restricted to the extracellular space and to action at the integrin—effectively slowed tumor growth and reduced vascularity [17, 18, 19, 20, 21]. The nanoparticle in this agent is biodegradable poly (lactic-co-glycolic acid) (PLGA). The antitumor effectiveness of NDAT involves pro-apoptotic activity and disruption of transcription of genes essential to a number of cancer cell survival pathways. The anti-angiogenic activity of NDAT involves disordering by several mechanisms of actions of endogenous growth factors, such as vascular endothelial growth factor (VEGF) , basic fibroblast growth factor (bFGF; FGF2)  and platelet-derived growth factor (PDGF) (S.A. Mousa, unpublished observations). NDAT also downregulates expression of the epidermal growth factor receptor (EGFR) gene . Again, all of these actions are nongenomically initiated at integrin αvβ3.
In the present studies, we document the efficacy of systemic NDAT, acting via the thyroid hormone-tetrac receptor on integrin αvβ3 against human U87MG glioblastoma xenografts.
Materials and Methods
Cultured U87MG-luc Cells
Human glioblastoma U87MG-luc cells were a generous gift from MD Anderson Cancer Center, Houston, TX, and were grown in DMEM supplemented with 10% fetal bovine serum, 1% penicillin, and 1% streptomycin. Cells were cultured at 37 °C to sub-confluence and treated with 0.25% (w/v) trypsin/EDTA to effect cell release from culture flask. Cells were washed with culture medium, suspended in DMEM that was free of phenol red and fetal bovine serum, and counted. Medium and other culture materials were from Sigma-Aldrich (St. Louis, MO).
Immunodeficient, female NCr nude homozygous mice aged 5–6 weeks and weighing between 18 and 20 g were purchased from Envigo (Indianapolis, IN). All animal studies were conducted at the animal facility of the Veteran Affairs Medical Center, Albany, NY, in accordance with and approved by institutional guidelines for humane animal treatment and according to the current guidelines. Mice were maintained under specific pathogen-free conditions and housed under controlled conditions of temperature (20–24 °C) and humidity (60–70%) and 12-h light/dark cycle with ad libitum access to water and food. Mice were allowed to acclimatize for 5 days prior to the start of study.
Tetrac was obtained from KareBay Biochem, Inc. (Monmouth Junction, NJ) and solubilized as previously described [19, 20], and NDAT was generated as previously described . Both chemical structures are shown in the Supplemental Data. The nanoparticle diameter distribution, morphology, and zeta potential have also been reported . The product consists of tetrac that is ether-bonded to a diaminoproprane linker via the outer ring hydroxyl group of tetrac. The linker is then attached by an amide bond to a nanoparticle of PLGA of approximately 150–200 nm. The agent is administered subcutaneously (s.c.) as a suspension in PBS. The amount of tetrac, itself, that is administered in NDAT is corrected for the contributions to molecular weight of the linker and PLGA nanoparticle.
In the first set of experiments, there were two discrete xenografts/animal and four animals in each of six experimental groups (control, void nanoparticle, tetrac (3 μg), tetrac (10 μg), NDAT (3 μg), NDAT (10 μg)). Cancer cells (2 × 106), together with the respective control or treatment compound, were implanted s.c. in each flank of each animal. The control was PBS, and treatment compounds were void nanoparticle (volume = 10 μg NDAT dose), unmodified tetrac (3 or 10 μg), or NDAT (3 or 10 μg). NDAT at 10 μg/implant achieves an intratumoral tetrac equivalent concentration of approximately 10−7 M . After humane sacrifice of animals at 16 days, tumors were harvested and hemoglobin concentration determined (see method below) to estimate graft vascularity. Tumor cell viability was estimated with In Vivo Imaging System (IVIS) scanning (see method, below).
In the second set of experiments, there were two grafts/animal and four animals for each experimental condition (control, NDAT). Xenografts consisted of 2 × 106 cancer cells implanted s.c. in each flank of each mouse. After 2 days, the animals were treated daily with control (PBS) or NDAT (1 mg/kg) s.c. for 10 days. Animals were then humanely sacrificed and harvested tumors were subjected to histopathology examination.
Estimation of Hemoglobin Content
Graft vascularity in the harvested tumors was estimated from an angiogenesis index of tumor cell lysate (tumor hemoglobin, mg/dL) measured with Drabkin’s reagent (Sigma-Aldrich) and with a hemoglobin standard, as described previously .
Estimation of Tumor Cells’ Viability
Viability of cells in situ in harvested tumors from U87MG-luc cell-grafted animals was determined with luminescent signal measurement in an IVIS® apparatus (PerkinElmer Inc., Waltham, MA).
Histopathology assessment of morphologic evidence of cell necrosis and apoptosis was done for slides prepared from the harvested tumors. Harvested xenografts were fixed in formalin, embedded in paraffin, and sectioned at the Wadsworth Center Core Histology Laboratory, New York State Department of Health. Paraffin-embedded tissue sections were stained with hematoxylin and eosin (H&E). Each tissue section was coded and examined by a board-certified pathologist who had no knowledge of the treatment exposure of the tissue (= blinded interpretation). The area of the tissue section was measured with a stage micrometer and the percentage of viable vs. necrotic tumor was estimated visually. The number of mitoses and apoptotic cells per high-power field was counted for five fields of viable tumor areas and averaged per tissue section. The degree of vascularization varied in the viable areas and this was graded numerically 1 to 4.
Estimation of Tumor Volume and Weight
Tumor width and length were estimated with calipers at 3-day intervals and volume calculated from the standard formula (W × L2/2). Tumor weight was measured in harvested lesions following humane sacrifice of animals.
Statistical analysis was performed using one-way ANOVA, comparing the mean ± SEM from each experimental group with its relevant control group. Statistical differences at p < 0.05 were considered significant.
Effect of Tetrac/NDAT Injected Intratumorally at Time of Implant on GBM Xenografts
For a measurement of tumor vascularity, the hemoglobin content of cell extracts of xenografts revealed that NDAT treatment resulted in a 50% loss of tumor blood vessel content (Fig. 1b).
Effect of Tetrac/NDAT Administered s.c. Daily on Established GBM Xenografts
Tumor Weight and Volume
There were no examples of intratumoral hemorrhage in xenografts from drug-treated or control animals, and animal weights over the 10-day treatment period were unaffected by NDAT administration (data not shown).
A variety of chemotherapeutic [26, 27, 28] and anti-angiogenic  approaches have been used to manage GBM clinically. Success has been limited and a number of new chemotherapeutic and immunotherapeutic strategies are under development [30, 31, 32, 33, 34]. Further, the introduction of treatment agents directly by a catheter into tumors [35, 36, 37, 38] offers the prospect of achieving high local concentrations of drug, bypass of the blood-brain barrier—although the latter may be porous about tumors [39, 40]—and limitation of systemic drug toxicity. Because of inherent radioresistance of this tumor, agents that radiosensitize are also of particular interest in management of glioblastoma.
In the present study, we determined the effectiveness of systemic NDAT (Nanotetrac, Nano-diamino-tetrac) against glioblastoma cell xenografts. The agent reduced tumor size promptly, effectively devascularized the tumors, and induced necrosis—presumably reflecting the loss of graft vascular supply—and apoptosis in cells not undergoing necrosis. Consistent with these findings, cell density in tumors from treated animals was reduced. In contrast to actions of other anti-angiogenic drugs tested oncologically [41, 42, 43], NDAT did not induce hemorrhage in the tumors or hemorrhagic events elsewhere. The basis of this finding in NDAT-exposed animals is not clear, but we propose that the effects on angiogenesis regulated from integrin αvβ3 can include systematic takedown of vasculature and not only inhibition of new blood vessel formation.
Cell necrosis in the context of devascularized tumors was expected. That apoptosis that was also induced by NDAT was also anticipated, given the existing evidence that NDAT is pro-apoptotic [14, 23]. The agent appears to affect both the intrinsic and extrinsic pathways of apoptosis.
The reduction in mitotic figures in tumors harvested from NDAT-treated animals is primarily a function of loss of cell viability. However, the drug is known to downregulate from its target/receptor on αvβ3 the transcription of a number of genes important to regulation of cell division [23, 44, 45].
In earlier in vitro studies, we showed that three rodent glioma cell lines proliferated in response to thyroid hormone and that this proliferative effect was blocked by tetrac . T3 and T4 were equipotent in these experiments, but free T4 concentrations in human subjects are 50-fold those of free T3, so that the responsiveness of GBM to thyroid hormone, dictated by the hormone receptor site on integrin αvβ3, is T4 based. NDAT inhibits binding of T4 and T3 to the integrin as one mechanism of antitumor action, but NDAT has a number of antitumor properties that are independent of agonist thyroid hormone, as was pointed out above. In addition to rodent glioma studies, we have also reported that a human GBM cell line (U87MG) proliferates when thyroid hormone is added to the medium in amounts that produce a directly measured physiologic level of free hormone . This hormonal action is mediated by mitogen-activated protein kinase (MAPK; ERK1/2).
Beyond anti-proliferation at the level of the tumor cell, a second important facet of the properties of NDAT is that it is anti-angiogenic by multiple mechanisms . This should be particularly relevant to GBM because of its extensive vascularity. NDAT inhibits actions of vascular endothelial growth factor (VEGF) [22, 46], basic fibroblast growth factor (bFGF) , platelet-derived growth factor (PDGF) (S.A. Mousa, unpublished observations), and epidermal growth factor (EGF) . Depending on the growth factor, these effects can involve gene transcription, growth factor release, or inhibitory crosstalk between the thyroid hormone-tetrac receptor on integrin αvβ3 and the vascular growth factor receptors clustered with the integrin on or in the plasma membrane.
A third facet of NDAT actions is that the agent increases radiosensitivity of human glioblastoma cells in vitro . This has not been examined in xenografts. The radiosensitization action of NDAT involves inhibition of repair of double-stranded DNA breaks in the tumor cell.
Finally, the PD-1 (programmed death-1)/PD-L1 (PD-ligand 1) immune checkpoint is affected by physiological concentrations of T4, in that the hormone stimulates expression in a variety of cell lines of the PD-L1 gene . NDAT blocks this effect. This checkpoint is a focus of interest in immunotherapy of GBM .
What is apparent from the present studies is that NDAT has a panel of important anticancer and anti-angiogenic actions on glioblastoma xenografts. These effects are nongenomically induced at a cell surface target expressed generously by cancer cells and dividing endothelial cells. The agent is not cytotoxic and limitation of its actions to tumor and blood vessel cells explains a favorable side effect profile in preclinical studies. That is, histologic examination of organs such as the brain, heart, liver, and kidney in rodents exposed to high-dose NDAT for weeks has shown no abnormalities (S.A. Mousa, S. Sell, unpublished observations). We would also point out that the use of anti-angiogenic agents in GBM clinical management increases the risk of intratumoral hemorrhage [51, 52]. Despite the multifactorial anti-angiogenic properties of Nanotetrac, no hemorrhages occurred in the xenografts of Nanotetrac-treated animals in the present study.
A limitation of the current work is that it was carried out on xenografts of a single, widely used human glioblastoma cell line. On the other hand, we have previously shown that rat C6 and F98 glioma cell lines and mouse GL261 glioma cells proliferate in response to T4 and that this hormonal action on these cell lines is blocked by tetrac . Further, human glioblastoma clinically responds to withdrawal of thyroid hormone [11, 53]. These observations are consistent with the NDAT observations we report in the current paper. The current studies were conducted on subcutaneous xenografts. We have compared the uptake of Cy5-labeled Nanotetrac in short-term (hours) by orthotopic and subcutaneous xenografts of U87-luc cells and have confirmed that tumoral uptake across the blood-brain barrier and in subcutaneous lesions is comparable (T. Sudha, D.J. Bharali, S.A. Mousa, unpublished observations).
The work reported here was supported in part by a grant from NanoPharmaceuticals LLC, Rensselaer, NY.
Compliance with Ethical Standards
All animal studies were conducted at the animal facility of the Veteran Affairs Medical Center, Albany, NY, in accordance with and approved by institutional guidelines for humane animal treatment and according to the current guidelines.
Conflict of Interest
Co-authors Davis and Mousa are stockholders in NanoPharmaceuticals LLC that is commercially developing NDAT (Nanotetrac, Nano-diamino-tetrac) and Davis is an officer of the company. All remaining authors have no conflicts to declare.
- 6.Chaichana KL, Cabrera-Aldana EE, Jusue-Torres I, Wijesekera O, Olivi A, Rahman M, Quinones-Hinojosa A (2014) When gross total resection of a glioblastoma is possible, how much resection should be achieved? World Neurosurg 82(1–2):e257–e265. doi: 10.1016/j.wneu.2014.01.019 CrossRefPubMedGoogle Scholar
- 11.Hercbergs AA, Goyal LK, Suh JH, Lee S, Reddy CA, Cohen BH, Stevens GH, Reddy SK, Peereboom DM, Elson PJ, Gupta MK, Barnett GH (2003) Propylthiouracil-induced chemical hypothyroidism with high-dose tamoxifen prolongs survival in recurrent high grade glioma: a phase I/II study. Anticancer Res 23(1B):617–626PubMedGoogle Scholar
- 12.Davis FB, Tang HY, Shih A, Keating T, Lansing L, Hercbergs A, Fenstermaker RA, Mousa A, Mousa SA, Davis PJ, Lin HY (2006) Acting via a cell surface receptor, thyroid hormone is a growth factor for glioma cells. Cancer Res 66(14):7270–7275. doi: 10.1158/0008-5472.CAN-05-4365 CrossRefPubMedGoogle Scholar
- 13.Bergh JJ, Lin HY, Lansing L, Mohamed SN, Davis FB, Mousa S, Davis PJ (2005) Integrin αvβ3 contains a cell surface receptor site for thyroid hormone that is linked to activation of mitogen-activated protein kinase and induction of angiogenesis. Endocrinology 146(7):2864–2871. doi: 10.1210/en.2005-0102 CrossRefPubMedGoogle Scholar
- 15.Lin HY, Tang HY, Keating T, Wu YH, Shih A, Hammond D, Sun M, Hercbergs A, Davis FB, Davis PJ (2008) Resveratrol is pro-apoptotic and thyroid hormone is anti-apoptotic in glioma cells: both actions are integrin and ERK mediated. Carcinogenesis 29(1):62–69. doi: 10.1093/carcin/bgm239 CrossRefPubMedGoogle Scholar
- 16.Lin HY, Sun M, Tang HY, Lin C, Luidens MK, Mousa SA, Incerpi S, Drusano GL, Davis FB, Davis PJ (2009) L-thyroxine vs. 3,5,3′-triiodo-l-thyronine and cell proliferation: activation of mitogen-activated protein kinase and phosphatidylinositol 3-kinase. Am J Physiol Cell Physiol 296(5):C980–C991. doi: 10.1152/ajpcell.00305.2008 CrossRefPubMedGoogle Scholar
- 17.Mousa SA, Yalcin M, Bharali DJ, Meng R, Tang HY, Lin HY, Davis FB, Davis PJ (2012) Tetraiodothyroacetic acid and its nanoformulation inhibit thyroid hormone stimulation of non-small cell lung cancer cells in vitro and its growth in xenografts. Lung Cancer 76(1):39–45. doi: 10.1016/j.lungcan.2011.10.003 CrossRefPubMedGoogle Scholar
- 18.Yalcin M, Bharali DJ, Dyskin E, Dier E, Lansing L, Mousa SS, Davis FB, Davis PJ, Mousa SA (2010a) Tetraiodothyroacetic acid and tetraiodothyroacetic acid nanoparticle effectively inhibit the growth of human follicular thyroid cell carcinoma. Thyroid 20(3):281–286. doi: 10.1089/thy.2009.0249 CrossRefPubMedGoogle Scholar
- 20.Yalcin M, Dyskin E, Lansing L, Bharali DJ, Mousa SS, Bridoux A, Hercbergs AH, Lin HY, Davis FB, Glinsky GV, Glinskii A, Ma J, Davis PJ, Mousa SA (2010b) Tetraiodothyroacetic acid (tetrac) and nanoparticulate tetrac arrest growth of medullary carcinoma of the thyroid. J Clin Endocrinol Metab 95(4):1972–1980. doi: 10.1210/jc.2009-1926 CrossRefPubMedGoogle Scholar
- 23.Davis PJ, Glinsky GV, Lin H-Y, Leith JT, Hercbergs A, Tang H-Y, Ashur-Fabian O, Incerpi S, Mousa SA (2014) Cancer cell gene expression modulated from plasma membrane integrin αvβ3 by thyroid hormone and nanoparticulate tetrac. Front Endocrinol (Lausanne) 5:240. doi: 10.3389/fendo.2014.00240 Google Scholar
- 25.Lin HY, Landersdorfer CB, London D, Meng R, Lim CU, Lin C, Lin S, Tang HY, Brown D, Van Scoy B, Kulawy R, Queimado L, Drusano GL, Louie A, Davis FB, Mousa SA, Davis PJ (2011) Pharmacodynamic modeling of anti-cancer activity of tetraiodothyroacetic acid in a perfused cell culture system. PLoS Comput Biol 7(2):e1001073. doi: 10.1371/journal.pcbi.1001073 CrossRefPubMedPubMedCentralGoogle Scholar
- 26.Drean A, Goldwirt L, Verreault M, Canney M, Schmitt C, Guehennec J, Delattre JY, Carpentier A, Idbaih A (2016) Blood-brain barrier, cytotoxic chemotherapies and glioblastoma. Expert Rev Neurother:1–16. doi: 10.1080/14737175.2016.1202761
- 31.Peschillo S, Caporlingua A, Diana F, Caporlingua F, Delfini R (2016) New therapeutic strategies regarding endovascular treatment of glioblastoma, the role of the blood-brain barrier and new ways to bypass it. J Neurointerv Surg 8(10):1078–1082. doi: 10.1136/neurintsurg-2015-012048 CrossRefPubMedGoogle Scholar
- 38.Vogelbaum MA, Sampson JH, Kunwar S, Chang SM, Shaffrey M, Asher AL, Lang FF, Croteau D, Parker K, Grahn AY, Sherman JW, Husain SR, Puri RK (2007) Convection-enhanced delivery of cintredekin besudotox (interleukin-13-pe38qqr) followed by radiation therapy with and without temozolomide in newly diagnosed malignant gliomas: phase 1 study of final safety results. Neurosurgery 61(5):1031–1037 . doi: 10.1227/01.neu.0000303199.77370.9ediscussion 1037-1038CrossRefPubMedGoogle Scholar
- 48.Shih A, Zhang S, Cao HJ, Tang HY, Davis FB, Davis PJ, Lin HY (2004) Disparate effects of thyroid hormone on actions of epidermal growth factor and transforming growth factor-alpha are mediated by 3′,5′-cyclic adenosine 5′-monophosphate-dependent protein kinase II. Endocrinology 145(4):1708–1717. doi: 10.1210/en.2003-0742 CrossRefPubMedGoogle Scholar
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